RecallRadar

FDA Device recall Z-1579-2022

Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Green: a) 25 pack, REF H93869025, b) 100 pack, REF H938674100, c) 100 pack, REF…

On 2022-08-31 the FDA classified a Class II recall of Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Green: a) 25 pack, REF H93869025, b) 100 pack, REF H938674100, c) 100 pack, REF… by Baxter Healthcare, citing there is a potential of the packaging not maintaining a sterile barrier for the tip caps.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1579-2022
ClassificationClass II
Statusongoing
Initiated2022-07-22
Published2022-08-31
Last updated2026-09-13 11:56 UTC
CompanyBaxter Healthcare
DistributionUS

Product

Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Green: a) 25 pack, REF H93869025, b) 100 pack, REF H938674100, c) 100 pack, REF H93869100

Reason

There is a potential of the packaging not maintaining a sterile barrier for the tip caps.

Identifiers

code_info
a) 25 pack, REF H93869025, UDI 00085412479965, ALL LOTS; b) 100 pack, REF H938674100, UDI 00085412479811, ALL LOTS; c…a) 25 pack, REF H93869025, UDI 00085412479965, ALL LOTS; b) 100 pack, REF H938674100, UDI 00085412479811, ALL LOTS; c) 100 pack, REF H93869100, UDI 00085412478944, ALL LOTS

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1579-2022%22

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